52858-01

GUDID 00885556909317

Cup Impactor - Straight

Smith & Nephew, Inc.

Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00885556909317
NIH Device Record Keyee63160e-02be-4f06-b39a-4819c0d61c6c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number52858-01
Catalog Number52858-01
Company DUNS045483575
Company NameSmith & Nephew, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556909317 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OLOOrthopedic stereotaxic instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


[00885556909317]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-16
Device Publish Date2025-05-08

Devices Manufactured by Smith & Nephew, Inc.

00885556903421 - EVOS2025-09-10 EVOS PELVIC 5.0MM X 135MM CANNULATED SCREW FULLY THREADED
00885556903438 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 140MM CANNULATED SCREW FULLY THREADED
00885556903445 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 145MM CANNULATED SCREW FULLY THREADED
00885556903452 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 150MM CANNULATED SCREW FULLY THREADED
00885556903469 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 50MM CANNULATED SCREW PARTIALLY THREADED 32MM
00885556903476 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 55MM CANNULATED SCREW PARTIALLY THREADED 32MM
00885556903483 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 60MM CANNULATED SCREW PARTIALLY THREADED 32MM
00885556903490 - EVOS2025-09-08 EVOS PELVIC 5.0MM X 65MM CANNULATED SCREW PARTIALLY THREADED 32MM

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